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Efficiency Clinical Study of NOVATEX MEDICAL Compression Garments in Patients With Ehlers-Danlos Syndrome — NOVASED  

Ehlers-Danlos Syndrome Clinical Trial

Official title:
Efficiency Clinical Study of NOVATEX MEDICAL Compression Garments in Patients With Ehlers-Danlos Syndrome

Clinical Trial Summary

Objective of this study is to assess the efficiency of NOVATEX MEDICAL compression garments in patients with an Ehlers-Danlos syndrome (EDS). To answer this objectif a comparison before/after use of compression garments will be performed for all patients.

Clinical Trial Description

Inclusion period: 1 year Follow-up period: 26 months Study period : 38 months Patient visits will be organized as follow: - V0: first visit at inclusion, clinical evaluation - V1: 4 months after inclusion, clinical evaluation without compression garments and presure garments prescription - V2: 8 months after inclusion, clinical evaluation with compression garments - V3: 14 months after inclusion, clinical evaluation with compression garments - V4: 20 months after inclusion, clinical evaluation with compression garments - V5: 26 months after inclusion, clinical evaluation with compression garments Only the first two visits are specific to the study to be able to compare before and after the use of compression garments. Next visits are the usual visits (every 6 months) for the use of compression garments in patients with an EDS. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03330977
Study type Interventional
Source Novatex Medical
Contact
Status Active, not recruiting
Phase N/A
Start date December 21, 2017
Completion date March 31, 2023
View Details
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